Related gene-specific medical variations for Gene (Select 386680) - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289627	NM_198694.3(KRTAP10-5):c.477G>T (p.Gln159His)	KRTAP10-5, TSPEAR (Q159H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289626	NM_198694.3(KRTAP10-5):c.238G>A (p.Ala80Thr)	KRTAP10-5, TSPEAR (A80T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3289625	NM_198694.3(KRTAP10-5):c.113C>A (p.Thr38Asn)	KRTAP10-5, TSPEAR (T38N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116877	NM_198694.3(KRTAP10-5):c.757C>T (p.Arg253Cys)	KRTAP10-5, TSPEAR (R253C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116876	NM_198694.3(KRTAP10-5):c.649C>T (p.Pro217Ser)	KRTAP10-5, TSPEAR (P217S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116875	NM_198694.3(KRTAP10-5):c.648A>T (p.Arg216Ser)	KRTAP10-5, TSPEAR (R216S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116874	NM_198694.3(KRTAP10-5):c.587C>T (p.Ser196Phe)	KRTAP10-5, TSPEAR (S196F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116873	NM_198694.3(KRTAP10-5):c.529T>C (p.Cys177Arg)	KRTAP10-5, TSPEAR (C177R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116872	NM_198694.3(KRTAP10-5):c.355A>G (p.Thr119Ala)	KRTAP10-5, TSPEAR (T119A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116871	NM_198694.3(KRTAP10-5):c.353C>T (p.Pro118Leu)	KRTAP10-5, TSPEAR (P118L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116870	NM_198694.3(KRTAP10-5):c.142T>C (p.Ser48Pro)	KRTAP10-5, TSPEAR (S48P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652767	NM_198694.3(KRTAP10-5):c.172C>T (p.Pro58Ser)	KRTAP10-5, TSPEAR (P58S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2598004	NM_198694.3(KRTAP10-5):c.610A>T (p.Ser204Cys)	KRTAP10-5, TSPEAR (S204C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541975	NM_198694.3(KRTAP10-5):c.265T>G (p.Cys89Gly)	KRTAP10-5, TSPEAR (C89G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523732	NM_198694.3(KRTAP10-5):c.35C>T (p.Ala12Val)	KRTAP10-5, TSPEAR (A12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463665	NM_198694.3(KRTAP10-5):c.142T>A (p.Ser48Thr)	KRTAP10-5, TSPEAR (S48T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460891	NM_198694.3(KRTAP10-5):c.518A>G (p.Tyr173Cys)	KRTAP10-5, TSPEAR (Y173C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2459795	NM_198694.3(KRTAP10-5):c.772G>A (p.Val258Met)	KRTAP10-5, TSPEAR (V258M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392926	NM_198694.3(KRTAP10-5):c.511T>G (p.Ser171Ala)	KRTAP10-5, TSPEAR (S171A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386995	NM_198694.3(KRTAP10-5):c.730G>A (p.Ala244Thr)	KRTAP10-5, TSPEAR (A244T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352847	NM_198694.3(KRTAP10-5):c.212C>T (p.Pro71Leu)	KRTAP10-5, TSPEAR (P71L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325459	NM_198694.3(KRTAP10-5):c.220T>G (p.Cys74Gly)	KRTAP10-5, TSPEAR (C74G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289854	NM_198694.3(KRTAP10-5):c.205T>G (p.Cys69Gly)	KRTAP10-5, TSPEAR (C69G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1695032	NM_198694.3(KRTAP10-5):c.267C>T (p.Cys89=)	KRTAP10-5, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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Links from Gene

Items: 24